Safety, Effectiveness and Patient Acceptance of the Treatment With MabCampath in Chronic Lymphocytic Leukemia

NCT00836043 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 6

Last updated 2013-12-03

No results posted yet for this study

Summary

This study will collect data on safety, effectiveness and patient acceptance of MabCampath treatment under daily life conditions.

Conditions

Interventions

DRUG

Alemtuzumab (MabCampath)

Intravenous therapy according to product information.

Sponsors & Collaborators

  • Genzyme, a Sanofi Company

    lead INDUSTRY

Principal Investigators

  • Medical Monitor · Genzyme, a Sanofi Company

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-10-31
Primary Completion
2009-04-30
Completion
2009-04-30

Countries

  • Bosnia and Herzegovina
  • Israel
  • North Macedonia

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00836043 on ClinicalTrials.gov